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MeSH keywords -> Related genes, diseases (OMIM)


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01 Ocular Hypertension [NCBI]


Gene


Gene Link Information
Gain
01
MYOC [NCBI] 0.0001621
OPTN [NCBI] 7.64535e-05
GFAP [NCBI] 2.19209e-05
FOXC1 [NCBI] 1.71713e-05
NEFM [NCBI] 1.69413e-05
NEFL [NCBI] 1.39619e-05
BDNF [NCBI] 1.35324e-05
OLFM2 [NCBI] 1.31586e-05
NEFH [NCBI] 1.26675e-05
NRN1 [NCBI] 1.21414e-05
NGF [NCBI] 1.0285e-05
GPNMB [NCBI] 9.80752e-06
RAB6A [NCBI] 9.53611e-06
LMX1B [NCBI] 9.37647e-06
RLBP1 [NCBI] 7.89267e-06
ACHE [NCBI] 7.42046e-06
STMN1 [NCBI] 6.92059e-06
OPA1 [NCBI] 6.88486e-06
HSD11B2 [NCBI] 6.83264e-06
NOS2 [NCBI] 6.72155e-06
NR3C1 [NCBI] 6.06169e-06
CYP1B1 [NCBI] 5.56713e-06
BMP4 [NCBI] 5.43517e-06
CCL5 [NCBI] 5.23173e-06
CNTF [NCBI] 4.76349e-06
IL1A [NCBI] 4.73395e-06
CCR5 [NCBI] 4.36047e-06
MMP2 [NCBI] 4.30705e-06
UMOD [NCBI] 4.2773e-06
CCR2 [NCBI] 4.26628e-06
TTR [NCBI] 4.01291e-06
MOG [NCBI] 3.69415e-06
CCL2 [NCBI] 3.45981e-06
IL1B [NCBI] 3.39949e-06
ACE [NCBI] 2.87575e-06
SOD1 [NCBI] 2.79868e-06
MBP [NCBI] 2.22731e-06
AR [NCBI] 1.77183e-06
VEGFA [NCBI] 1.6026e-06
APOE [NCBI] 1.41512e-06
PTH [NCBI] 9.60128e-07




OMIM


OMIM Link Information
gain
01
glaucoma-related pigment dispersion syndrome [NCBI] 0.00141831
VRNI [NCBI] 0.00120335
OPTN [NCBI] 0.000357694
MYOC [NCBI] 0.000355641
POAG [NCBI] 0.000265517
glaucoma, normal tension, susceptibility to [NCBI] 0.000221079
GLC1A [NCBI] 0.000162014
IRID1 [NCBI] 8.95027e-05
infantile spasm syndrome, x-linked [NCBI] 8.21852e-05
XFS [NCBI] 8.21852e-05
GFAP [NCBI] 8.17471e-05
OPA1 [NCBI] 7.1734e-05
NPS [NCBI] 5.92212e-05
osteogenesis imperfecta, type i [NCBI] 5.58533e-05
BDNF [NCBI] 5.17307e-05
OPA1 [NCBI] 4.48047e-05
NGFB [NCBI] 3.28366e-05
COL1A1 [NCBI] 2.9718e-05
ACHE [NCBI] 2.46381e-05
RP [NCBI] 2.33451e-05
CNTF [NCBI] 1.81562e-05
AR [NCBI] 4.1218e-06
APOE [NCBI] 3.58223e-06
VEGF [NCBI] 9.18656e-07
PTH [NCBI] 4.09112e-07




Database Center for Life Science